What pattern of curved arrow pushing is the second step of this reaction? O₂N. O₂N H O proton transfer O loss of leaving group O nucleophilic attack O rearrangement
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- OH + H* Under what condition would the reaction proceed faster? O A. In the presence of a salt O B. Acid-base mixture catalyzed O. Base catalyzed O D. Acid catalyzedWhat is the intermediate before the final product of the following reactions? ii NaOH H* heat O a. Na Ob. OH OH Od. Na* он e. Of.Which bond breaks in the given reaction? A or B?
- :Draw two major products :Reaction type for the major product :Draw one minor product :Reaction type for the minor productHow is this reaction classified? R DG TXI Reaction progress Free energy з O a Endergonic O b. Electrophilic Addition Oc. Nucleophilic Addition O d. Exergonic PCould the reactions shown here take place by a concerted mechanism?
- S. Classify the following reagents as either nucleophiles or electrophiles: Znt, CH,NH2, HS, OH, , CH,COOH, H,SO,Draw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. H N. Br2 Br • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one. IZPlease don't provide handwriting solution
- For the following reaction: Br HO. a-Explain how to decide which mechanism(s) the reaction will follow including o alkyl halide substitution o nucleophile or base strength o solvent b-State which mechanism(s) will occur. c-Draw the product(s).By taking into account electronegativity differences, draw the products formed by heterolysis of the carbon–heteroatom bond in each molecule. Classify the organic reactive intermediate as a carbocation or a carbanion.Draw an energy diagram of the following reactions. A one step reaction with a positive AG A one step reaction with a negative AG A two-step reaction with an overall positivel-Where the intermediates are lower energy than the reactants and the first transition state is lower in energy than the second.